Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
  • C08K3/06—Sulfur
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L21/00—Compositions of unspecified rubbers

Definitions

• This invention relates to styrene-sulfur compounds and more particularly, to a novel Class of reaction products of styrene and sulfur that are especially useful in the vulcanization of rubbers.
• styrene and sulfur can be reacted at temperatures of the order of 150 C. to produce viscous liquid'products having sulfur ranks of the order of 1 to 5.
• Sulfur rank as the term is used in this art is the ratio of the moles of sulfur in the product to moles of organic monomeric units, e.g., styrene units, in the product. It is further known that such liquid sulfur-bearing products may be used in place of elemental sulfur in the vulcanization of rubbers and that when so used they provide certain advantages over the use of sulfur per se.
• liquid styrene-sulfur polymers as vulcanizing agents for rubber leads to certain advantages as outlined above, their use as vulcanizing agents is subject to a number of disadvantages in comparison with the results achieved with elemental sulfur.
• a viscous liquid such as the liquid styrene-sulfur polymers mentioned above
• the organic portion of the styrene-sulfur polymer tends to exert a plasticizing effect on the rubber, thus producing a softer vulcanizate for a given quantity of available sulfur in the curing agent.
• Other objects of the invention will be in part obvious and in part pointed out hereafter.
• the present invention is predicated on the findings that by reacting styrene and sulfur in suitable proportions under suitable reaction conditions, it is possible to produce a class of solid polymeric products having sulfur ranks within the range 10 to 25 and softening temperatures substantially below that of elemental sulfur.
• These products have a relatively high available sulfur content, with the result that they can be used in relativelysmall amounts in the vulcanization of rubber.
• they since they have a relatively low organic content and can be used in small amounts, they have a much smaller plasticizing effect upon the rubber in which they are incorporate-d than do the liquid styrene-sulfur compounds of the prior art.
• the products are sufliciently friable so that they can be readily reduced to a fine powder and incorporated in the rubber using the standard milling techniques common in the rubber industry. Also they have greater bloom-resistance than elemental sulfur.
• the products of the present invention can be prepared by mixing styrene and sulfur in the proportions of 10 to 25 moles of sulfur per mole of styrene monomer and heating the mixture at a temperature of to 135 C. for a period of five to thirty hours.
• Polymeric addition products are formed under these conditions which, upon cooling'to room temperature, form friable solids having, as indicated above, a high proportion of available sulfur when used as vulcanizing agents for rubber.
• the products can be used to vulcanize any of the sulfur-vulcanizable rubbers including natural rubher and synthetic rubbery materials having aliphatic unsaturation.
• Rubbers of this type include natural rubber, butadiene 1,3-styrene copolymers, butadiene 1,3-acrylonitrile copolymers, polybutadienes, polyisoprenes, and polychloroprenes. They may be substituted for sulfur in standard vulcanizing formulations and when used in the proportions of 1%-4% by weight, based on the weight of the rubber, give vulcanizates having excellent tensile and elastic properties. Since they are friable solids, they can be readily reduced to powder form and incorporated in the rubber by the usual milling techniques. Curing is effected by heating at temperatures of say 250 F. to 325 F.
• the present compounds Because of the less drastic heating cycle made possible by the use of the present compounds, less deterioration of the rubber occurs and hence improved physical properties can be obtained.
• the present compounds have a high available sulfur content, they are more efficient than the liquid sulfur-styrene products of the prior art. That is to say, they can be used in smaller amounts and introduce into the vulcanizate a smaller portion of the styrene radicals which as noted above tend to plasticize and soften the vulcanizate.
• Preferred results have been obtained by using styrene-sulfur polymers having a sulfur rank of about 15.
• Example I A reaction vessel was charged with 100 moles (3206 grams) of sulfur and 10 moles (1041 grams) of inhibited styrene, and the atmosphere above the mixture of styrene and sulfur was purged with nitrogen. The mixture was agitated and heated at C. for 6.5 hours, during which time nitrogen was bubbled through the reaction mixture. The resulting composition-Was a dark brown solid polymer having a sulfur rank of 10 and a sulfur content of 3 about 74% by weight. The polymer solidified upon coolmg at room temperature in about 70 hours.
• Example 11 A reaction vessel was charged with 15 moles (481 grams) of sulfur and 1 mole (104 grams) of inhibited styrene, and the atmosphere above the mixture of styrene and sulfur was purged with nitrogen. The mixture was agitated and heated at a temperature of 125 C. for 30 hours during which time nitrogen was bubbled through the reaction mixture. At the end of 30 hours the resulting composition was a dark viscous polymer having a sulfur rank of 15 and a sulfur content of about 82% by Weight. It was allowed to stand at room temperature for about 70 hours and cooled to form a brittle yellow solid having a softening point of about 157 F.
• Example 111 Twenty moles (641.2 grams) of sulfur and one mole (104.1 grams) of inhibited styrene were agitated and heated together to 125 C. in a nitrogen-purged atmosphere. The temperature was maintained at 125 C. for 10 hours during which time nitrogen was bubbled through the reaction'mixture. The resulting. composition was a dark viscous polymer having a sulfur rank of 20. The polymer solidified upon cooling at room temperature in about 70 hours.
• Example IV A mixture of moles (802 grams) of sulfur and 1 mole (104 grams) of inhibited styrene were heated under a nitrogen atmosphere as in Example I at a temperature
• Example V Two parts by weight of the styrene polysulfide polymer product of rank 10 produced as in Example I was compounded on a rubber mill with an unsaturated elastomeric rubber compound comprised of: 100 parts of GRS1502 Government Rubber Styrene composition commonly identified as SBR (styrene butadiene rubber), 50 parts HAP Black carbon black and 5 parts of Santocure accelerator, wherein all parts are by weight.
• SBR styrene butadiene rubber
• HAP Black carbon black 50 parts of Santocure accelerator, wherein all parts are by weight.
• HAF Black is a high abrasion furnace black and Santocure accelerator is N-cyclohexyl-Z-benzothiazole sulfenamide, sold by Monsanto Chemical Company.
• the resulting mixture after aging at room temperature for about 48 hours, was a vulcanizable rubber composition.
• the composition When subjected to the Mooney scorch resistance test, the composition exhibited a rise of 4 points in an excess of minutes. Press curing the composition at 300 F. for 40 minutes produced a vulcanized rubber material which when tested in accordance with ASTM D395 (Method B) procedure for rubber materials, had the following physical properties: compression set resistance of 72% after heating at 250 F. for 24 hours, and an initial compression of 25%; tensile strength of 3790 p.s.i.; 200% modulus of 1400 p.s.i.; elongation of 3.70%; and a Shore A hardness of 68.
• Example V1 Three parts by weight of a polysulfide polymer product of rank 10 produced as described in Example I above was compounded on a rubber mill with parts of the unsaturated elastomeric rubber compound described in Example V. The product, after aging at room temperature for about 48 hours, was a vulcanizable rubber compound. Testing and curing procedures used in this'example were the same as described in Example V, and they produced a vulcanized rubber material having the following physical properties: Mooney scorch resistance of 4 point rise in excess of 30 minutes; compression set resistance of 70%; tensile strength of 3390 p.s.i.; 200% modulus of 1580 p.s.i.; elongation of 340%; and a hardness of Shore A 71.
• Example VII Four parts by weight of a polysulfide polymer product of rank 10 produced as described in Example I was compounded on a rubber mill with 155 parts of the unsaturated elastomeric rubber compound described in Example V. The product, after aging at room temperatu're about 48 hours, was a vulcanizable rubber compound.
• Example V Testing and curing procedures used in this example were the same as described in Example V and resulted in a vulcanized rubber material having the fol lowing physical properties: Mooney scorch resistance of 4 point rise in excess of 30 minutes; compression set resistance of 71%; tensile strength of 3300 p.s.i.; 200% modulus of 2330 p.s.i.; elongation of 260%; and a hardness of Shore A 72.
• Example VIII Two parts by weight of the styrene polysulfide polymer of rank 15 produced as described in Example II, and more particularly Sample A of Example II, was compounded on a rubber mill with 155 parts of the unsaturated elastomeric rubber compound described in Example V. The product, after aging at room temperature for about 48 hours, was a vulcanizable rubber compound.
• Example V The testing and curing procedures used in this example were the same as described in Example V, and they resulted in a vulcanized rubber material having the following physical properties: Mooney scorch resistance of 4 point rise in excess of 30 minutes; compression set resistance of 62%; tensile strength of 3820 p.s.i.; 200% modulus of 1950 p.s.i.; elongation of 300%; and a hardness of Shore A 71.
• Example IX Twlo parts by weight of the styrene polysulfide polymer of rank 15 produced as described in Example II, and more particularly, Sample B of Example II, was compounded on a rubber mill with 155 parts of the unsaturated elastomeric rubber compound of Example V.
• Example V After aging at room temperature about 48 hours, wasja vulcanizable rubber compound.
• the testing and curing procedures used in this example were the same as described in Example V, and they resulted in a vulcanized rubber material having the following physical properties:
• Example X rubber material having the following physical properties: Mooney scorch resistance of 4 point rise in excess of 30 minutes; compression set resistance of 60%; tensile strength of 4100 p.s.i.; 200% modulus of 2000 p.s.i.; elongation of 350%; and a hardness of Shore A 70.
• Example XI Two parts by weight of the sulfur-styrene polymer of rank as produced in Example II above, and more particularly, Sample A of Example II, was compounded on a rubber mill with an unsaturated elastomeric rubber compound comprised of: 100 parts by weight of butadienestyrene rubber (Philprene 1502 produced by Phillips Petroleum Co.), 15 parts of HAF Black carbon black, 5 parts of zinc oxide, 1 part of stearic acid, and 1.25 parts of Santocure accelerator. The resulting mixture was aged at room temperature for about 48 hours and was then ready for vulcanization.
• an unsaturated elastomeric rubber compound comprised of: 100 parts by weight of butadienestyrene rubber (Philprene 1502 produced by Phillips Petroleum Co.), 15 parts of HAF Black carbon black, 5 parts of zinc oxide, 1 part of stearic acid, and 1.25 parts of Santocure accelerator.
• the resulting mixture was aged at room temperature for about 48 hours and was then ready for vulcan
• a composition as thus prepared was tested in various ways to determine its properties. It was found that when the composition was subjected to the Mooney scorch resistance test, it exhibited a rise of 4 points in excess of 30 minutes. When the composition was press cured at 300 F. for 40 minutes, it produced a vulcanized rubber having the following properties: compression set resistance of 62%; tensile strength of 3830 p.s.i.; 200% modulus of 1950 p.s.i.; elongation of 300%; Shore A hardness of 71. The polymer used in this formulation provides an especially good balance of curing performance and non-blooming characteristics.
• Example XII Two parts by weight of the polysulfied polymer product of rank produced in Example 111 was compounded on a rubber mill with 155 parts of the unsaturated elastomeric rubber compound described in Example V. The product, after aging at room temperature for about 48 hours, was a vulcanizable rubber compound. Testing and curing procedures used in this example were the same as described in Example V, and they resulted in a vulcanized rubber material having the following physical properties: Mooney scorch resistance of 4 point rise in excess of 30 minutes; compression set resistance of 58%; tensile strength of 3800 p.s.i.; 200% modulus of 1740 p.s.i.; elongation of 350%; and a hardness of Shore A 70.
• Example XIII Two parts by weight of the styrene-sulfur polymer of the rank produced as described in Example IV was compounded on a rubber mill with 122.25 parts of the unsaturated rubber compound of Example XI. The milled product was aged at room temperature for about 48 hours and tested using the test procedures of Example V. Its
• the present invention provides a novel group of solid styrene-sulfur compounds that are exceptionally useful as vulcanizing agents for rubbers.
• These solid vulcanizing agents eliminate a number of the disadvantages of elemental sulfur and the liquid styrene-sulfur products of the prior art while at the same time combining the advantages of both of these prior vulcanizing agents.
• the foregoing examples are illustrative only and that numerous changes can be made in the ingredients, proportions, and conditions spe cifically set forth therein without departing from the spirit of the invention as set forth in the appended claims.
• a method of making a friable solid polymer of styrene which comprises heating a mixture of styrene and sulfur wherein the molar ratio of sulfur to styrene is from 10 to 25 at a temperature of to C. to form said solid polymer.
• the method of producing a vulcanized rubber which comprises mixing a sulfur-vulcanizable rubber with from 1% to 4% by weight based on the weight of said rubbery material, of a solid styrene-sulfur polymer having a sulfur rank of from 10 to 25, and curing the resulting mixture at a temperature of from about 250 to about 325 F.
• a vulcanizable rubbery composition comprising a major proportion of a sulfur-vulcanizable rubber and from 1 to 4% by weight, based on the weight of said rubber, of a styrene-sulfur polymer having a sulfur rank of from 10 to 25.

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• Chemical & Material Sciences (AREA)
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• Compositions Of Macromolecular Compounds (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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  • NL NL283424D patent/NL283424A/xx unknown
  • BE BE623102D patent/BE623102A/xx unknown
• 1961
  • 1961-10-06 US US143308A patent/US3231546A/en not_active Expired - Lifetime
• 1962
  • 1962-09-25 CH CH1124862A patent/CH410429A/de unknown
  • 1962-10-04 DE DET22822A patent/DE1223558B/de active Pending
  • 1962-10-05 GB GB37768/62A patent/GB956338A/en not_active Expired

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